Coping With Charcot-Marie-Tooth DiseaseThis section is a place to share stories about Coping With Charcot-Marie-Tooth Disease Below are entries of those who have already shared their stories. We hope that you find their experiences helpful to your own situation. You may also Help others by sharing your story. To quickly access health information from your website's browser, download charcot marie tooth disease i was diagnosed with cmt 6 years ago and have really noticed how much it has really started to affect me things like standing in 1 spot seem to be such a chore for me these days im only 21 and theres so many things that i want to do but my feet are the things stopping me in my quality of life each day to be is starting to become such a chore and when i meet new ppl i try to hide the way i walk i used to be really active played netball soccer and i was a good runner but things like going for a walk around the block are such a chore these days i really hate it and it really frustrates me so much that i cant do what most ppl take for granted im lucky though in one aspect it hasnt affected my hands or arms yet but what i hate the most is i no nobody in my situaqtion were im from and im so sick of being on crutches all the time i just wish that i could live a normal life Comments
September 2007
|
|
Archives:
The submissions from our site visitors do not reflect the opinion of Healthcommunities.com, Inc. (HC). The Content of HC's sites is intended for informational and educational purposes only, and is not intended to be a substitute for professional medical advice, diagnosis, or treatment. HC does not provide medical advice. Never disregard professional medical advice or delay seeking it because of something you've read on an HC website. Always seek the advice of your physician or other qualified health care provider regarding any medical question or condition. (See also: Website Disclaimer) |

